Term Name: hereditary spastic paraplegia 44
Synonyms: autosomal recessive spastic paraplegia 44, SPG44
Definition: A hereditary spastic paraplegia that has_material_basis_in mutation in the GJC2 gene on chromosome 1q42.
Ontology: Human Disease [DOID:0110796]   ( DOID:0110796 )

Relationships
is a type of: autosomal recessive disease hereditary spastic paraplegia